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Complex Chemistry pp 51–152Cite as

Nature and dynamics of the spin-state interconversion in metal complexes

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Part of the book series: Structure and Bonding ((STRUCTURE,volume 76))

Abstract

Spin-state transitions in metal complexes which are driven by a change of temperature T or pressure p are always associated with a considerable reorganization of molecular geometry. The change involves metal-ligand bond lengths R, bond angles, and a variation of ligand orientation. In particular, the elongation 4R by up to ∼ 10% occurring in the course of the LS → HS conversion produces an expansion of molecular volume ΔV ≌ 25 Å3 per metal atom. The average crystal structure for given values of T and p is reproduced by the fractional occupancy of the individual structures of the high-spin (HS) and low-spin (LS) isomer. The transitions are reasonably well described by a number of theoretical models which are equivalent to the Bragg and Williams approximation of the Ising model. The dynamics of the spin-state transitions in solution, based on measurements by ultrasonic and photo-perturbation techniques, is in general rapid with rate constants between 4 × 105 and 3 × 108 s−1. Similar results are obtained for the spin conversion in solid complexes where the line shape analysis of Mössbauer spectra based on the theory of Blume and Tjon is applied. The dynamics may be rationalized employing one-dimensional cross sections through Gibbs free-energy surfaces G = G(R), an alternative being the comparison of the results with quantum-mechanical calculations for a radiationless non-adiabatic multiphonon process.

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  1. Institut für Physikalische and Theoretische Chemie, University of Erlangen-Nürnberg, D-8520, Erlangen, Germany

    Edgar König

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König, E. (1991). Nature and dynamics of the spin-state interconversion in metal complexes. In: Complex Chemistry. Structure and Bonding, vol 76. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-53499-7_2

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